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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Copper-Catalyzed Regioselective Allylic Cyanation of Allylic Compounds with Trimethylsilyl Cyanide
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Copper-Catalyzed Regioselective Allylic Cyanation of Allylic Compounds with Trimethylsilyl Cyanide

机译:用三甲基甲硅烷基氰化物的铜催化的烯丙基化合物的区域染色剂

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摘要

The copper-catalyzed regioselective allylic cyanation of allylic compounds with trimethylsilyl cyanide (TMSCN) is described. Copper(I) iodide (Cul), copper(I) cyanide (CuCN) and cop-per(II) chloride (CuCl_2) are shown to effectively catalyze the cyanation of various allylic substrates to afford the corresponding allylic cyanides in good yields and high regioselectivities. The reaction in the presence of 2,2,6,6-tetramethyl-l-piperidinyloxy free radical (TEMPO) reveals that the cyanation proceeds via a radical pathway.
机译:描述了用三甲基甲硅烷基氰化物(TMSCN)的铜催化的烯丙基化合物的烯丙基灭菌。 铜(I)碘化铜(CUL),铜(I)氰化物(CUCN)和COP-/每II)氯化物(CUCL_2)有效地催化各种烯丙基底物的氰化物,以良好的产率和高产生相应的烯丙基氰化物 区域选择性。 在2,2,6,6-四甲基-1-哌啶氧基氧基(Tempo)存在下的反应表明,氰化术通过自由基途径进行。

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